Clearance Summary
DIAMOND BLADE MICROMETER KNIFE received FDA 510(k) clearance under submission number K860332, sponsored by Med-Tech Develoment Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1986-02-13.
- Submission: K860332
- Applicant / Sponsor: Med-Tech Develoment Corp.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class I
- Regulation citation: 21 CFR 886.4350
- Decision date: 1986-02-13
Classification & Regulation
This clearance is catalogued under FDA product code HNN and 21 CFR 886.4350, within the Ophthalmic review panel as a Class I device.